Research Coordinator II - Pulmonary COPD
Houston Methodist
At Houston Methodist, the Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study.
FLSA STATUS
ExemptQUALIFICATIONS
EDUCATION
Bachelor’s degreeEXPERIENCE
Four years of research experienceLICENSES AND CERTIFICATIONS
CCRC - Certified Clinical Research Coordinator (ACRP) CCRP - Certified Clinical Research Professional (SOCRA)SKILLS AND ABILITIES
Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on‑going skills, competency assessments, and performance evaluations Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles Ability to work independently Capable of handling challenging/difficult situations Demonstrates sound judgment and executes above‑average analytical skillsESSENTIAL FUNCTIONS
PEOPLE ESSENTIAL FUNCTIONS
Under the direction of the Principal Investigator (PI), drafts various communications with the Sponsor and/or regulatory documents to be sent to the Sponsor. Identifies and recruits clinical research subjects and monitors enrollment goals. May conduct in‑services to floor nurses/physicians; assists in precepting new clinical research staff and educating other research staff regarding scientific aspects of studies. Teaches peers to critically think by verbally expressing rationale for decisions and follows up consistently. Uses peer‑to‑peer accountability towards improvement of department score for turnover/retention/employee engagement.SERVICE ESSENTIAL FUNCTIONS
Participates in the Principal Investigator (PI) meetings. Schedules, coordinates, and participates in the pre‑site visit and site initiation visits; coordinates study initiation. Obtains Informed Consent from study participant and documents appropriately. Obtains vital signs and performs phlebotomy per training and competence; monitors participants’ labs and notifies the PI of laboratory findings.QUALITY/SAFETY ESSENTIAL FUNCTIONS
Prepares Institutional Research Board (IRB) documents under the direction of the PI, assists with answering IRB stipulations to obtain final approval; documents IRB approval and contract approval. Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process. Adheres to internal controls established for the department.FINANCE ESSENTIAL FUNCTIONS
Assists with the budget development and Medicare coverage analysis. Utilizes resources effectively and efficiently, demonstrating responsible financial stewardship. Manages own time effectively and prioritizes work to achieve maximum results in a timely manner.GROWTH/INNOVATION ESSENTIAL FUNCTIONS
Assists PI and/or research nurse in the planning and design of source documents for protocol. Assists in developing procedures for laboratory collection and storage. Incorporates directions from other health care disciplines into clinical research protocols when reviewing patient eligibility; assists in eliciting relevant data from sources outside of the hospital. Proactively manages own professional development and completes My Development Plan.SUPPLEMENTAL REQUIREMENTS
WORK ATTIRE
Uniform: No Scrubs: Yes Business professional: No Other (department approved): YesON‑CALL
*Note that employees may be required to be on‑call during emergencies (ie. Disaster, Severe Weather Events, etc) regardless of selection below. On Call* NoTRAVEL
Travel specifications may vary by department May require travel within the Houston Metropolitan area No May require travel outside Houston Metropolitan area No Houston Methodist is an Equal Opportunity Employer. #J-18808-Ljbffr Houston Methodist- Houston Methodist is hiring a Research Coordinator II in St. Louis, Missouri, responsible for the coordination of day-to-day research activities and ensuring the accuracy of data collection related to clinical research. The ideal candidate should possess a Bachelor’s degree...Suggested
$52.6k - $78.9k
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...the clinic, and the Study to Understand Novel Biomarkers in Researching Dementia (SUNBIRD) validates blood biomarkers for Alzheimer’s... ...multidisciplinary research team and performs duties associated with the coordination and implementation of research studies/projects, data...Work experience placementWork at office- Washington University is seeking a Research Nurse Coordinator II for the Vascular Surgery department. This full-time position involves coordinating research projects and providing direct patient care. Responsibilities include supervising staff, managing clinical trials,...Full time
$60k - $90k
...to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we... ...is better and more accessible for all. The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices...Full timeTemporary workWork at officeLocal areaWorldwideVisa sponsorshipWork visaRelocation packageFlexible hours$52.6k - $78.9k
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